Nasdaq Hearing Panel Grants AnPac Bio’s Request to Transfer Securities from The Nasdaq Global Market to The Nasdaq Capital Market
06 May 2022 - 09:30PM
GlobeNewswire Inc.
AnPac Bio-Medical Science Co., Ltd. (“AnPac Bio,” the “Company” or
“we”) (ANPC), a biotechnology company with operations in the United
States and China focused on early cancer screening and detection,
announced that the Nasdaq Hearings Panel (the “Panel”) has granted
the request of AnPac Bio to transfer the Company’s American
Depositary Shares from The Nasdaq Global Market to The Nasdaq
Capital Market, effective May 6, 2022 and to continue its listing
on The Nasdaq Stock Market, subject to various conditions. The
Nasdaq Capital Market has lower listing requirements than those of
The Nasdaq Global Market, while both are a part of The Nasdaq Stock
Market.
Under the terms of the decision, the Panel has
stated that on or before May 31, 2022, the Company must evidence
compliance with The Nasdaq Capital Market’s $2.5 million
stockholder’s equity requirement, by filing a Form 6-K with the
U.S. Securities and Exchange Commission, containing: 1) a
description of the completed transactions or events that enabled
the Company to satisfy the stockholder’s equity requirement for
continued listing; and 2) a balance sheet, no older than 60 days
with pro forma adjustments for any significant transactions or
events occurring on or before the report date, which evidences
compliance with the stockholders’ equity requirement; and 3) a
disclosure that the Company believes it also satisfies the
stockholders’ equity requirement as of the report date. The
transfer to The Nasdaq Capital Market does not resolve the dollar
bid requirement, which remains outstanding.
In order to fully comply with the terms of this
decision, the Company must be able to demonstrate compliance with
all applicable requirements for continued listing on The Nasdaq
Capital Market by May 31, 2022. In that regard, the Company is
currently in a grace period for the $1 bid price requirement that
runs through September 5, 2022. As a result, the Company does not
have to regain compliance with the bid price requirement in order
to satisfy the decision. Companies listed on The Nasdaq Capital
Market may be eligible for a second 180-day grace period for bid
price if they meet certain standards, including a demonstration
that stockholders’ equity is at least $5 million. In the event the
Company is unable to meet the terms of the decision, the Company
may seek a further extension from the Panel not to exceed September
20, 2022; however, there can be no assurance that the Panel would
grant a further extension or that the Company will return to
compliance.
About AnPac Bio
AnPac Bio is a biotechnology company focused on
early cancer screening and detection, with 150 issued patents as of
September 30, 2021. With two certified clinical laboratories in
China and one CLIA and CAP accredited clinical laboratory in the
United States, AnPac Bio performs a suite of cancer screening and
detection tests, including CDA (Cancer Differentiation Analysis),
bio-chemical, immunological, and genomics tests. According to
a report by Frost & Sullivan, AnPac Bio ranked first globally
in multi-cancer screening and detection test sample volume
(accumulative to January 2021). AnPac Bio’s CDA
technology platform has been shown in retrospective validation
studies to be able to detect the risk of over 20 different cancer
types with high sensitivity and specificity.
For more information, please
visit: https://www.Anpacbio.com.
For investor and media inquiries, please
contact:
Company:
Phil Case, Marketing and Investor RelationsPhone:
+1-267-810-6776 (US)Email: phil_case@AnPacbio.com
Investor Relations:
Ascent Investor Relations LLCTina Xiao, PresidentPhone:
+1-917-609-0333
(US)Email: tina.xiao@ascent-ir.com
Safe Harbor Statement
This announcement contains forward-looking
statements within the meaning of Section 27A of the Securities Act
of 1933 and Section 21E of the Securities Exchange Act of 1934.
These forward-looking statements are made under the “safe harbor”
provisions of the Private Securities Litigation Reform Act of 1995
and are relating to the Company’s future financial and operating
performance. The Company has attempted to identify forward-looking
statements by terminologies including “believes,” “estimates,”
“anticipates,” “expects,” “plans,” “projects,” “intends,”
“potential,” “target,” “aim,” “predict,” “outlook,” “seek,” “goal”
“objective,” “assume,” “contemplate,” “continue,” “positioned,”
“forecast,” “likely,” “may,” “could,” “might,” “will,” “should,”
“approximately” or other words that convey uncertainty of future
events or outcomes to identify these forward-looking statements.
These statements are based on current expectations, assumptions and
uncertainties involving judgments about, among other things, future
economic, competitive and market conditions and future business
decisions, all of which are difficult or impossible to predict
accurately and many of which are beyond the Company’s control.
These statements also involve known and unknown risks,
uncertainties and other factors that may cause the Company’s actual
results to be materially different from those expressed or implied
by any forward-looking statement. Known and unknown risks,
uncertainties and other factors include, but are not limited to,
our ability to comply with Nasdaq Listing Rules, the implementation
of our business model and growth strategies; trends and competition
in the cancer screening and detection market; our expectations
regarding demand for and market acceptance of our cancer screening
and detection tests and our ability to expand our customer base;
our ability to obtain and maintain intellectual property
protections for our CDA technology and our continued research and
development to keep pace with technology developments; our ability
to obtain and maintain regulatory approvals from the NMPA, the FDA
and the relevant U.S. states and have our laboratories certified or
accredited by authorities including the CLIA; our future business
development, financial condition and results of operations and our
ability to obtain financing cost-effectively; potential changes of
government regulations; general economic and business conditions in
China and elsewhere; our ability to hire and maintain key
personnel; our relationship with our major business partners and
customers; and the duration of the coronavirus outbreaks and their
potential adverse impact on the economic conditions and financial
markets and our business and financial performance, such as
resulting from reduced commercial activities due to quarantines and
travel restrictions instituted by China, the U.S. and many other
countries around the world to contain the spread of the virus.
Additionally, all forward-looking statements are subject to the
“Risk Factors” detailed from time to time in the Company’s most
recent Annual Report on Form 20-F and other filings with the U.S.
Securities and Exchange Commission. Because of these and other
risks, uncertainties and assumptions, undue reliance should not be
placed on these forward-looking statements. In addition, these
statements speak only as of the date of this press release and,
except as may be required by law, the Company undertakes no
obligation to revise or update publicly any forward-looking
statements for any reason.
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